Composition and adaptation of human myotendinous junction and neighboring muscle fibers to heavy resistance training

Scand J Med Sci Sports. 2017 Dec;27(12):1547-1559. doi: 10.1111/sms.12794. Epub 2016 Oct 26.

Abstract

The myotendinous junction (MTJ) is a common site of strain injury and yet understanding of its composition and ability to adapt to loading is poor. The main aims of this study were to determine the profile of selected collagens and macrophage density in human MTJ and adjoining muscle fibers, and to investigate whether heavy exercise loading would alter this profile. Fifteen individuals scheduled for anterior cruciate ligament repair surgery were randomized into three groups: control, acute or 4 weeks heavy resistance training. MTJ samples were collected from the semitendinosus and gracilis muscles and were sectioned and stained immunohistochemically for collagen types I, III, VI, XII, XIV, XXII, Tenascin-C and CD68. Macrophage density and distribution was evaluated and the amount of each collagen type in muscle and MTJ was graded. Collagen XXII was observed solely at the MTJ, while all other collagens were abundant at the MTJ and in muscle perimysium or endomysium. The endomysial content of collagen XIV, macrophages and Tenascin-C increased following 4 weeks of training. These findings illustrate the heterogeneity of collagen type composition of human MTJ. The increase in collagen XIV following 4 weeks of training may reflect a training-induced protection against strain injuries in this region.

Keywords: Injury prevention; Nordic Hamstring; extracellular matrix.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Adaptation, Physiological*
  • Adult
  • Anterior Cruciate Ligament Injuries / surgery
  • Antigens, CD / physiology
  • Antigens, Differentiation, Myelomonocytic / physiology
  • Collagen / physiology
  • Female
  • Humans
  • Macrophages / cytology
  • Male
  • Muscle Fibers, Skeletal / physiology*
  • Resistance Training*
  • Tenascin / physiology
  • Tendons / physiology*

Substances

  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • CD68 antigen, human
  • Tenascin
  • Collagen